| 臺大學術典藏 |
2020-12-01T08:29:03Z |
Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
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Bentley A.R.; Sung Y.J.; Brown M.R.; Winkler T.W.; Kraja A.T.; Ntalla I.; Schwander K.; Chasman D.I.; Lim E.; Deng X.; Guo X.; Liu J.; Lu Y.; Cheng C.-Y.; Sim X.; Vojinovic D.; Huffman J.E.; Musani S.K.; Li C.; Feitosa M.F.; Richard M.A.; Noordam R.; Baker J.; Chen G.; Aschard H.; Bartz T.M.; Ding J.; Dorajoo R.; Manning A.K.; Rankinen T.; Smith A.V.; Tajuddin S.M.; Zhao W.; Graff M.; Alver M.; Boissel M.; Chai J.F.; Chen X.; Divers J.; Evangelou E.; Gao C.; Goel A.; Hagemeijer Y.; Harris S.E.; Hartwig F.P.; He M.; Horimoto A.R.V.R.; Hsu F.-C.; Hung Y.-J.; Jackson A.U.; Kasturiratne A.; Komulainen P.; Kühnel B.; Leander K.; Lin K.-H.; Luan J.; Lyytikäinen L.-P.; Matoba N.; Nolte I.M.; Pietzner M.; Prins B.; Riaz M.; Robino A.; Said M.A.; Schupf N.; Scott R.A.; Sofer T.; Stancáková A.; Takeuchi F.; Tayo B.O.; van der Most P.J.; Varga T.V.; TZUNG-DAU WANG; Wang Y.; Ware E.B.; Wen W.; Xiang Y.-B.; Yanek L.R.; Zhang W.; Zhao J.H.; Adeyemo A.; Afaq S.; Amin N.; Amini M.; Arking D.E.; Arzumanyan Z.; Aung T.; Ballantyne C.; Barr R.G.; Bielak L.F.; Boerwinkle E.; Bottinger E.P.; Broeckel U.; Brown M.; Cade B.E.; Campbell A.; Canouil M.; Charumathi S.; Chen Y.-D.I.; Christensen K.; Concas M.P.; Connell J.M.; de las Fuentes L.; de Silva H.J.; de Vries P.S.; Doumatey A.; Duan Q.; Eaton C.B.; Eppinga R.N.; Faul J.D.; Floyd J.S.; Forouhi N.G.; Forrester T.; Friedlander Y.; Gandin I.; Gao H.; Ghanbari M.; Gharib S.A.; Gigante B.; Giulianini F.; Grabe H.J.; Gu C.C.; Harris T.B.; Heikkinen S.; Heng C.-K.; Hirata M.; Hixson J.E.; Ikram M.A.; Jia Y.; Joehanes R.; Johnson C.; Jonas J.B.; Justice A.E.; Katsuya T.; Khor C.C.; Kilpeläinen T.O.; Koh W.-P.; Kolcic I.; Kooperberg C.; Krieger J.E.; Kritchevsky S.B.; Kubo M.; Kuusisto J.; Lakka T.A.; Langefeld C.D.; Langenberg C.; Launer L.J.; Lehne B.; Lewis C.E.; Li Y.; Liang J.; Lin S.; Liu C.-T.; Liu J.; Liu K.; Loh M.; Lohman K.K.; Louie T.; Luzzi A.; Mägi R.; Mahajan A.; Manichaikul A.W.; McKenzie C.A.; Meitinger T.; Metspalu A.; Milaneschi Y.; Milani L.; Mohlke K.L.; Momozawa Y.; Morris A.P.; Murray A.D.; Nalls M.A.; Nauck M.; Nelson C.P.; North K.E.; O’Connell J.R.; Palmer N.D.; Papanicolau G.J.; Pedersen N.L.; Peters A.; Peyser P.A.; Polasek O.; Poulter N.; Raitakari O.T.; Reiner A.P.; Renström F.; Rice T.K.; Rich S.S.; Robinson J.G.; Rose L.M.; Rosendaal F.R.; Rudan I.; Schmidt C.O.; Schreiner P.J.; Scott W.R.; Sever P.; Shi Y.; Sidney S.; Sims M.; Smith J.A.; Snieder H.; Starr J.M.; Strauch K.; Stringham H.M.; Tan N.Y.Q.; Tang H.; Taylor K.D.; Teo Y.Y.; Tham Y.C.; Tiemeier H.; Turner S.T.; Uitterlinden A.G.; van Heemst D.; Waldenberger M.; Wang H.; Wang L.; Wang L.; Wei W.B.; Williams C.A.; Wilson G.; Sr, Wojczynski M.K.; Yao J.; Young K.; Yu C.; Yuan J.-M.; Zhou J.; Zonderman A.B.; Becker D.M.; Boehnke M.; Bowden D.W.; Chambers J.C.; Cooper R.S.; de Faire U.; Deary I.J.; Elliott P.; Esko T.; Farrall M.; Franks P.W.; Freedman B.I.; Froguel P.; Gasparini P.; Gieger C.; Horta B.L.; Juang J.-M.J.; Kamatani Y.; Kammerer C.M.; Kato N.; Kooner J.S.; Laakso M.; Laurie C.C.; Lee I.-T.; Lehtimäki T.; Magnusson P.K.E.; Oldehinkel A.J.; Penninx B.W.J.H.; Pereira A.C.; Rauramaa R.; Redline S.; Samani N.J.; Scott J.; Shu X.-O.; van der Harst P.; Wagenknecht L.E.; Wang J.-S.; Wang Y.X.; Wareham N.J.; Watkins H.; Weir D.R.; Wickremasinghe A.R.; Wu T.; Zeggini E.; Zheng W.; Bouchard C.; Evans M.K.; Gudnason V.; Kardia S.L.R.; Liu Y.; Psaty B.M.; Ridker P.M.; van Dam R.M.; Mook-Kanamori D.O.; Fornage M.; Province M.A.; Kelly T.N.; Fox E.R.; Hayward C.; van Duijn C.M.; Tai E.S.; Wong T.Y.; Loos R.J.F.; Franceschini N.; Rotter J.I.; Zhu X.; Bierut L.J.; Gauderman W.J.; Rice K.; Munroe P.B.; Morrison A.C.; Rao D.C.; Rotimi C.N.; Cupples L.A.; COGENT-Kidney Consortium, EPIC-InterAct Consortium, Understanding Society Scientific Group, Lifelines Cohort |
| 臺大學術典藏 |
2020-11-25T07:22:53Z |
Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry
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Chen, C-Y J; Juang, J-M J; Lin, L-Y; Liu, Y-B; Ho, L-T; Yu, C-C; Huang, H-C; Lin, T-T; Liao, M-C; Chen, J-J; Hwang, J-J; Chen, W-J; Yeh, S-F S; Yang, D-H; Chiang, F-T; Lin, J-L; Lai, L-P; Horie, M |
| 臺大學術典藏 |
2020-11-17T02:45:34Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
|
Lin J.-L.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Hwang J.-J.; Juang J.-M.J.;Tzu-Pin Lu;Lai L.-C.;Hsueh C.-H.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;Yu C.-C.;Hwang J.-J.;Chiang F.-T.;Yeh S.S.-F.;Chen W.-P.;Chuang E.Y.;Lai L.-P.;Lin J.-L.; Juang J.-M.J.; TZU-PIN LU; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C. |
| 臺大學術典藏 |
2020-11-17T02:45:33Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
|
Chuang E.Y.; Lin J.-L.; Juang J.-M.J.;Tzu-Pin Lu;Lai L.-C.;Ho C.-C.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;Yu C.-C.;Chen W.-J.;Chiang F.-T.;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Lin J.-L.; Juang J.-M.J.; TZU-PIN LU; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Chen W.-J.; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P. |
| 臺大學術典藏 |
2020-11-17T02:45:26Z |
Genome-wide methylation profiles in coronary artery ectasia
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Chuang N.-C.; Cheng C.-Y.; Hsu C.-A.; Wang Y.-C.; Lin Y.-H.; Lee J.-K.; Wu C.-K.; Hwang J.-J.; Lin L.-Y.; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J.; Tzu-Pin Lu;Chuang N.-C.;Cheng C.-Y.;Hsu C.-A.;Wang Y.-C.;Lin Y.-H.;Lee J.-K.;Wu C.-K.;Hwang J.-J.;Lin L.-Y.;Yeh S.-F.S.;Chien K.-L.;Juang J.-M.J.; TZU-PIN LU |
| 臺大學術典藏 |
2020-11-17T02:45:24Z |
An automated microfluidic DNA microarray platform for genetic variant detection in inherited arrhythmic diseases
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Huang S.-H.;Chang Y.-S.;Juang J.-M.J.;Chang K.-W.;Tsai M.-H.;Tzu-Pin Lu;Lai L.-C.;Chuang E.Y.;Huang N.-T.; Huang S.-H.; Chang Y.-S.; Juang J.-M.J.; Chang K.-W.; Tsai M.-H.; TZU-PIN LU; Lai L.-C.; Chuang E.Y.; Huang N.-T. |
| 臺大學術典藏 |
2020-11-17T02:45:22Z |
VariED: The first integrated database of gene annotation and expression profiles for variants related to human diseases
|
Juang J.-M.J.; Lai L.-C.; Tsai M.-H.; TZU-PIN LU; Chuang E.Y.; Lee C.-Y.;Chattopadhyay A.;Chiang L.-M.;Juang J.-M.J.;Lai L.-C.;Tsai M.-H.;Tzu-Pin Lu;Chuang E.Y.; Lee C.-Y.; Chattopadhyay A.; Chiang L.-M. |
| 臺大學術典藏 |
2020-11-17T02:45:22Z |
Impact of ancestral differences and reassessment of the classification of previously reported pathogenic variants in patients with brugada syndrome in the genomic era: A SADS-TW BrS registry
|
Chen C.-Y.J.;Tzu-Pin Lu;Lin L.-Y.;Liu Y.-B.;Ho L.-T.;Huang H.-C.;Lai L.-P.;Hwang J.-J.;Yeh S.-F.S.;Wu C.-K.;Juang J.-M.J.;Antzelevitch C.; Chen C.-Y.J.; TZU-PIN LU; Lin L.-Y.; Liu Y.-B.; Ho L.-T.; Huang H.-C.; Lai L.-P.; Hwang J.-J.; Yeh S.-F.S.; Wu C.-K.; Juang J.-M.J.; Antzelevitch C. |
| 臺大學術典藏 |
2020-07-01T08:12:26Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
|
Juang J.-M.J.;Lu T.-P.;Liang-Chuan Lai;Hsueh C.-H.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;Yu C.-C.;Hwang J.-J.;Chiang F.-T.;Yeh S.S.-F.;Chen W.-P.;Chuang E.Y.;Lai L.-P.;Lin J.-L.; Juang J.-M.J.; Lu T.-P.; LIANG-CHUAN LAI; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Hwang J.-J.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L. |
| 臺大學術典藏 |
2020-07-01T08:12:23Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
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Juang J.-M.J.;Lu T.-P.;Liang-Chuan Lai;Ho C.-C.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;Yu C.-C.;Chen W.-J.;Chiang F.-T.;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Lin J.-L.; Juang J.-M.J.; Lu T.-P.; LIANG-CHUAN LAI; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Chen W.-J.; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Lin J.-L. |
| 臺大學術典藏 |
2020-07-01T08:12:15Z |
An automated microfluidic DNA microarray platform for genetic variant detection in inherited arrhythmic diseases
|
Huang S.-H.;Chang Y.-S.;Juang J.-M.J.;Chang K.-W.;Tsai M.-H.;Lu T.-P.;Liang-Chuan Lai;Chuang E.Y.;Huang N.-T.; Huang S.-H.; Chang Y.-S.; Juang J.-M.J.; Chang K.-W.; Tsai M.-H.; Lu T.-P.; LIANG-CHUAN LAI; Chuang E.Y.; Huang N.-T. |
| 臺大學術典藏 |
2020-06-29T01:21:30Z |
An automated microfluidic DNA microarray platform for genetic variant detection in inherited arrhythmic diseases
|
Huang, S.-H.;Chang, Y.-S.;Juang, J.-M.J.;Chang, K.-W.;Tsai, M.-H.;Lu, T.-P.;Lai, L.-C.;Chuang, E.Y.;Huang, N.-T.; Huang, S.-H.; Chang, Y.-S.; Juang, J.-M.J.; Chang, K.-W.; Tsai, M.-H.; Lu, T.-P.; Lai, L.-C.; Chuang, E.Y.; Huang, N.-T.; NIEN-TSU HUANG |
| 臺大學術典藏 |
2020-04-16T02:34:27Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
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Yeh, S.S.-F.; Chen, W.-P.; Chuang, E.Y.; Lai, L.-P.; Lin, J.-L.; ERIC YAO-YU CHUANG; Juang, J.-M.J.;Lu, T.-P.;Lai, L.-C.;Hsueh, C.-H.;Liu, Y.-B.;Tsai, C.-T.;Lin, L.-Y.;Yu, C.-C.;Hwang, J.-J.;Chiang, F.-T.;Yeh, S.S.-F.;Chen, W.-P.;Chuang, E.Y.;Lai, L.-P.;Lin, J.-L.; Juang, J.-M.J.; Lu, T.-P.; Lai, L.-C.; Hsueh, C.-H.; Liu, Y.-B.; Tsai, C.-T.; Lin, L.-Y.; Yu, C.-C.; Hwang, J.-J.; Chiang, F.-T. |
| 臺大學術典藏 |
2020-04-16T02:34:24Z |
Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation
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Tsai, C.-T.;Hsieh, C.-S.;Chang, S.-N.;Chuang, E.Y.;Juang, J.-M.J.;Lin, L.-Y.;Lai, L.-P.;Hwang, J.-J.;Chiang, F.-T.;Lin, J.-L.; Tsai, C.-T.; Hsieh, C.-S.; Chang, S.-N.; Chuang, E.Y.; Juang, J.-M.J.; Lin, L.-Y.; Lai, L.-P.; Hwang, J.-J.; Chiang, F.-T.; Lin, J.-L.; ERIC YAO-YU CHUANG |
| 臺大學術典藏 |
2020-03-03T03:06:30Z |
Myocardial Regional Interstitial Fibrosis is Associated with Left Intra-Ventricular Dyssynchrony in Patients with Heart Failure: A Cardiovascular Magnetic Resonance Study
|
Lin L.-Y.; Wu C.-K.; Juang J.-M.J.; Wang Y.-C.; Su M.-Y.M.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; WEN-YIH TSENG; Lin J.-L. |
| 臺大學術典藏 |
2020-02-27T07:42:50Z |
Prevalence of atrial fibrillation in patients with brugada syndrome in Taiwan
|
Liu Y.B.; Lin L.-Y.; WEN-JONE CHEN; Lai L.-P.; Tsai C.-T.; Lin J.-L.; Lin J.-L.;Tsai C.-T.;Lai L.-P.;WEN-JONE CHEN;Lin L.-Y.;Liu Y.B.;Chen C.-Y.;Juang J.-M.J.; Juang J.-M.J.; Chen C.-Y. |
| 臺大學術典藏 |
2020-02-27T07:42:47Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
|
Lin J.-L.;Chuang E.Y.;Lai L.-P.;Yeh S.-F.S.;Chiang F.-T.;WEN-JONE CHEN;Yu C.-C.;Lin L.-Y.;Tsai C.-T.;Liu Y.-B.;Ho C.-C.;Lai L.-C.;Lu T.-P.;Juang J.-M.J.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; WEN-JONE CHEN; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Lin J.-L. |
| 臺大學術典藏 |
2020-02-27T07:42:46Z |
Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan
|
Lin J.-L.;Lai L.-P.;Sherri Yeh S.-F.;Yeh H.-M.;Chiang F.-T.;Tseng C.-D.;WEN-JONE CHEN;Chiu F.-C.;Chen J.-J.;Hwang J.-J.;Yu C.-C.;Liu Y.-B.;Lin L.-Y.;Tsai C.-T.;Juang J.M.J.; Juang J.M.J.; Tsai C.-T.; Lin L.-Y.; Liu Y.-B.; Yu C.-C.; Hwang J.-J.; Chen J.-J.; Chiu F.-C.; WEN-JONE CHEN; Tseng C.-D.; Chiang F.-T.; Yeh H.-M.; Sherri Yeh S.-F.; Lai L.-P.; Lin J.-L. |
| 臺大學術典藏 |
2020-02-10T09:00:12Z |
VariED: the first integrated database of gene annotation and expression profiles for variants related to human diseases
|
Lee C.-Y.;Chattopadhyay A.;Chiang L.-M.;Juang J.-M.J.;Lai L.-C.;Tsai M.-H.;Lu T.-P.;Chuang E.Y.; Lee C.-Y.; Chattopadhyay A.; Chiang L.-M.; Juang J.-M.J.; Lai L.-C.; Tsai M.-H.; Lu T.-P.; Chuang E.Y.; MONG-HSUN TSAI |
| 臺大學術典藏 |
2020 |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
|
Juang J.-M.J.; TZU-PIN LU; Chen C.-Y.J.; Huang H.-C.; Ho L.-T.; Yu C.-C.; Lin L.-Y.; Binda A.; Lee S.-J.; Hwang J.-J.; Chen W.-J.; Liu Y.-B.; Antzelevitch C.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Juang J.-M.J.;Binda A.;Lee S.-J.;Hwang J.-J.;Chen W.-J.;Liu Y.-B.;Lin L.-Y.;Yu C.-C.;Ho L.-T.;Huang H.-C.;Chen C.-Y.J.;Tzu-Pin Lu;Lai L.-C.;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Rivolta I.;Antzelevitch C. |
| 臺大學術典藏 |
2020 |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
|
Binda A.; Juang J.-M.J.; Antzelevitch C.; Chuang E.Y.; Rivolta I.; Lee S.-J.; Hwang J.-J.; WEN-JONE CHEN; Liu Y.-B.; Lin L.-Y.; Yu C.-C.; Ho L.-T.; Huang H.-C.; Chen C.-Y.J.; Lu T.-P.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P. |
| 臺大學術典藏 |
2020 |
Application of the newest European Association of Cardiovascular Imaging Recommendation regarding the long-term prognostic relevance of left ventricular diastolic function in heart failure with preserved ejection fraction
|
Wu C.-K.; HWANG, JUEY-JEN; Juang J.-M.J.; Wang Y.-C.; Lin T.-T. |
| 臺大學術典藏 |
2020 |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
|
Chen, W.-J.; Lee, S.-J.; Hwang, J.-J.; Binda, A.; Juang, J.-M.J.; Juang, J.-M.J.;Binda, A.;Lee, S.-J.;Hwang, J.-J.;Chen, W.-J.;Liu, Y.-B.;Lin, L.-Y.;Yu, C.-C.;Ho, L.-T.;Huang, H.-C.;Chen, C.-Y.J.;Lu, T.-P.;Lai, L.-C.;Yeh, S.-F.S.;Lai, L.-P.;Chuang, E.Y.;Rivolta, I.;Antzelevitch, C.; SHYH-JYE LEE; Liu, Y.-B.; Lin, L.-Y.; Yu, C.-C.; Ho, L.-T.; Huang, H.-C.; Chen, C.-Y.J.; Lu, T.-P.; Lai, L.-C.; Yeh, S.-F.S.; Lai, L.-P.; Chuang, E.Y.; Rivolta, I.; Antzelevitch, C. |
| 臺大學術典藏 |
2019-11-27T06:54:13Z |
Fabry disease cardiac variant IVS4+919 G>A is associated with multiple cardiac gene variants in patients with severe cardiomyopathy and fatal arrhythmia
|
Juang J.-M.J.;Shun C.-T.;Yih-Sharng Chen;Hwu W.-L.;Lee N.-C.;Tsai W.-H.;Chen N.-Q.;Chien Y.-H.; Juang J.-M.J.; Shun C.-T.; YIH-SHARNG CHEN; Hwu W.-L.; Lee N.-C.; Tsai W.-H.; Chen N.-Q.; Chien Y.-H. |
| 臺大學術典藏 |
2019 |
Metabolomic analysis of platelets of patients with aspirin non-response
|
Chuang J.-Y.; Wu C.-K.; Lee S.-H.; Chen Y.-C.; Chiang J.-Y.; Chiang J.-Y.;Lee S.-H.;Chen Y.-C.;Wu C.-K.;Chuang J.-Y.;Shyh-Chyi Lo;Yeh H.-M.;Yeh S.-F.;Hsu C.-A.;Lin B.-B.;Chang P.-C.;Chang C.-H.;Liang H.-J.;Chiang F.-T.;Lin C.-Y.;Juang J.-M.J.; SHYH-CHYI LO; Yeh H.-M.; Yeh S.-F.; Hsu C.-A.; Lin B.-B.; Chang P.-C.; Chang C.-H.; Liang H.-J.; Chiang F.-T.; Lin C.-Y.; Juang J.-M.J. |
